{"title":"非水介质中某些取代铬衍生物在铂、金和玻碳电极上的电化学研究","authors":"A. E. Maghraby","doi":"10.2174/1876505X00901010008","DOIUrl":null,"url":null,"abstract":"The redox characteristics of some substituted chromene derivatives has been investigated in different nonaque- ous solvents such as, 1,2- dichloroethane (DCE), dichloromethane (DCM) and acetonitrile (AN) using 0.1mol dm -3 tetrabutylammonium perchlorate (TBAP) as a supporting electrolyte at platinum, gold and glassy carbon electrodes, using cyclic voltammetry. Through controlled potential electrolysis (CPE), the product of oxidation and reduction can be sepa- rated and identified. The product of oxidation was found to be the corresponding bis-compound. On the other hand, the reduction occurs in a single two electron process to give the dianion, which abstracts protons to saturate the (-C=O) bond. The effect of substituents on the redox mode of an electroactive site has also been studied.","PeriodicalId":23074,"journal":{"name":"The Open Electrochemistry Journal","volume":"31 1","pages":"8-14"},"PeriodicalIF":0.0000,"publicationDate":"2009-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Electrochemical Study of Some Substituted Chromene Derivatives in Nonaqueous Media at Pt, Au and Glassy Carbon Electrodes\",\"authors\":\"A. E. Maghraby\",\"doi\":\"10.2174/1876505X00901010008\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The redox characteristics of some substituted chromene derivatives has been investigated in different nonaque- ous solvents such as, 1,2- dichloroethane (DCE), dichloromethane (DCM) and acetonitrile (AN) using 0.1mol dm -3 tetrabutylammonium perchlorate (TBAP) as a supporting electrolyte at platinum, gold and glassy carbon electrodes, using cyclic voltammetry. Through controlled potential electrolysis (CPE), the product of oxidation and reduction can be sepa- rated and identified. The product of oxidation was found to be the corresponding bis-compound. On the other hand, the reduction occurs in a single two electron process to give the dianion, which abstracts protons to saturate the (-C=O) bond. The effect of substituents on the redox mode of an electroactive site has also been studied.\",\"PeriodicalId\":23074,\"journal\":{\"name\":\"The Open Electrochemistry Journal\",\"volume\":\"31 1\",\"pages\":\"8-14\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Open Electrochemistry Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/1876505X00901010008\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Open Electrochemistry Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1876505X00901010008","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Electrochemical Study of Some Substituted Chromene Derivatives in Nonaqueous Media at Pt, Au and Glassy Carbon Electrodes
The redox characteristics of some substituted chromene derivatives has been investigated in different nonaque- ous solvents such as, 1,2- dichloroethane (DCE), dichloromethane (DCM) and acetonitrile (AN) using 0.1mol dm -3 tetrabutylammonium perchlorate (TBAP) as a supporting electrolyte at platinum, gold and glassy carbon electrodes, using cyclic voltammetry. Through controlled potential electrolysis (CPE), the product of oxidation and reduction can be sepa- rated and identified. The product of oxidation was found to be the corresponding bis-compound. On the other hand, the reduction occurs in a single two electron process to give the dianion, which abstracts protons to saturate the (-C=O) bond. The effect of substituents on the redox mode of an electroactive site has also been studied.